A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529497



Internal ID305513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92149774..92149871hg38UCSC Ensembl
chr15:92693004..92693101hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703670
Samples
Known GenesSLCO3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529497
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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